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Acetic Acid → 5-(4-Bromophenyl)-1,2-oxazole-4-carboxylic acid

HRID 2391108
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인쇄 미리보기

반응식

HRID 2391108 반응식
C([O:3][C:4]([C:6]1[CH:7]=[N:8][O:9][C:10]=1[C:11]1[CH:16]=[CH:15][C:14]([Br:17])=[CH:13][CH:12]=1)=[O:5])C.C(O)(=O)C.O>Cl>[Br:17][C:14]1[CH:13]=[CH:12][C:11]([C:10]2[O:9][N:8]=[CH:7][C:6]=2[C:4]([OH:5])=[O:3])=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 962WaterHCID 22220993Ethyl 5-(4-bromophenyl)isoxazole-4-carboxylate

생성물 1

HCID 228317015-(4-Bromophenyl)-1,2-oxazole-4-carboxylic acid

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

5-(4-Bromo-phenyl)-isoxazole-4-carboxylic acid ethyl ester (0.500 g, 1.69 mmol) was dissolved in concentrated hydrochloric acid (2 mL), acetic acid (5 mL), and H2O (5 mL), and the reaction was stirred at 100° C. overnight. The mixture was partitioned between EtOAc and H2O, and the organic layer was separated, dried over MgSO4, filtered, and concentrated to give the title compound.

후처리

  1. customThe mixture was partitioned between EtOAc and H2O
  2. customthe organic layer was separated
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-bae1155603924c8ea866c158fa084018
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273780B2

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